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PFIZERPEN®Principal Display Panel (penicillin G potassium)

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Label

NDC 0049-0520-84
Rx only

Buffered
Pfizerpen®
(penicillin G potassium, USP)
For Injection

5,000,000 Units* per vial
(Five million units* per vial)

Intramuscular or Intravenous Use

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Label

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Carton

10 Vials
Buffered

NDC 0049-0520-83
Contains 10 of NDC 0049-0520-84
Rx only

Pfizerpen®
(penicillin G potassium, USP)
For Injection

5,000,000 Units* per vial
(Five million units* per vial)

Intramuscular or Intravenous Use

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Carton

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Label

NDC 0049-0530-28
Rx only

Buffered
Pfizerpen®
(penicillin G potassium, USP)

20,000,000 Units* per vial

(Twenty million units* per vial)
For Intravenous Infusion Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Label

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Carton

NDC 0049-0530-28
Rx only

1 Vial
Buffered

Pfizerpen®
(penicillin G potassium, USP)

20,000,000
Units*
per vial
(Twenty million units* per vial)

For Intravenous Infusion Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Carton
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Report Adverse Event
Pfizer Safety

To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

If you cannot use the above website or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at
(800) 438-1985.
FDA Medwatch
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatchor by calling
(800)-332-1088.